Development and validation of a computed tomography myocardial perfusion imaging radiomic model for major adverse cardiovascular events prediction: a multicenter study

European Heart Journal - Cardiovascular Imaging

6 February 2026
Organised by: Logo
ESC Journals CORONARY ARTERY DISEASE, ACUTE CORONARY SYNDROMES, ACUTE CARDIAC CARE IMAGING Cardiac Computed Tomography (CT)

Abstract

AbstractAims

Accurate prediction of major adverse cardiovascular events (MACE) is crucial for risk stratification in patients with suspected coronary artery disease. CT myocardial perfusion imaging (CT-MPI) provides various parameters, which may help comprehensively characterize perfusion features. This study aimed to develop a combined model, including clinical risk factors, coronary atherosclerotic characteristics, and radiomic features derived from CT-MPI, to predict MACE.

Methods and results

784 patients who underwent coronary CT angiography (CCTA) and CT-MPI from eight hospitals were retrospectively enrolled. Radiomic analysis was performed on eight perfusion parameter maps. Three prediction models were established accordingly: Model 1 (clinical risk factors and coronary atherosclerotic characteristics), Model 2 (incorporating myocardial blood flow values upon Model 1), and Model 3 (integrating radiomic scores upon Model 2). The C-indices for Model 3 in the training, internal validation, and external validation sets were 0.898 (95% confidence interval [CI]: 0.856–0.947), 0.844 (95% CI: 0.780–0.908), and 0.840 (95% CI: 0.791–0.889), respectively, demonstrating significant improvements over Model 1 and Model 2 (all P < 0.05). In the external validation set, Model 3 had the largest time-dependent areas under the curve (AUC) values for 1-, 3-, and 5-year MACE prediction (0.890 [95% CI: 0.831–0.948], 0.880 [95% CI: 0.823–0.938], and 0.837 [95% CI: 0.726–0.949]), compared with Model 1 and Model 2.

Conclusion

The radiomic features from multiparametric CT-MPI maps simultaneously captured perfusion features associated with MACE at both macrovascular and microvascular levels. The combined model exhibited improved MACE prognostic performance compared with conventional models while maintaining high interpretability.

ESC 365 is supported by